Enhanced microbial electrosynthesis with three-dimensional graphene functionalized cathodes fabricated via solvothermal synthesis

2016 ◽  
Vol 217 ◽  
pp. 117-122 ◽  
Author(s):  
Nabin Aryal ◽  
Arnab Halder ◽  
Pier-Luc Tremblay ◽  
Qijin Chi ◽  
Tian Zhang
2016 ◽  
Vol 72 (1) ◽  
pp. 80-83 ◽  
Author(s):  
Cameron Black ◽  
Philip Lightfoot

VIVoxyfluorides are of interest as frustrated magnets. The successful synthesis of two-dimensionally connected vanadium(IV) oxyfluoride structures generally requires the use of ionic liquids as solvents. During solvothermal synthesis experiments aimed at producing two- and three-dimensional vanadium(IV) selenites with triangular lattices, the title compound, diaquatetra-μ-fluorido-dioxidodivanadium(IV) monohydrate, V2O2F4(H2O)2·H2O, was discovered and features a new infinite V4+-containing two-dimensional layer comprised of fluorine-bridged corner- and edge-sharing VOF4(H2O) octahedral building units. The synthesis was carried out under solvothermal conditions. The V4+centre exhibits a typical off-centring, with a short V=O bond and an elongatedtrans-V—F bond. Hydrogen-bonded water molecules occur between the layers. The structure is related to previously reported vanadium oxyfluoride structures, in particular, the same layer topology is seen in VOF3.


2020 ◽  
Vol 4 (1) ◽  
pp. 337-346 ◽  
Author(s):  
Hailiang Chu ◽  
Ying Zhu ◽  
Tingting Fang ◽  
Junqiang Hua ◽  
Shujun Qiu ◽  
...  

CoNi LDH-6 with a nano-petal structure was prepared, which exhibited excellent rate performance and long-term stability as a supercapacitor electrode.


2014 ◽  
Vol 2 (32) ◽  
pp. 13093-13102 ◽  
Author(s):  
Ludovic Jourdin ◽  
Stefano Freguia ◽  
Bogdan C. Donose ◽  
Jun Chen ◽  
Gordon G. Wallace ◽  
...  

Enhanced performance for the bioelectrosynthesis of acetate from carbon dioxide is achieved with a new three-dimensional CNT-modified scaffold electrode.


2020 ◽  
Vol 98 (7) ◽  
pp. 365-372
Author(s):  
Matthew L. Brown ◽  
Daniel B. Leznoff

The solvothermal synthesis and characterization of a three-dimensional, interpenetrated uranyl dicyanoaurate coordination polymer, K2(UO2)2(UO2)2(Au(CN)2)2(O)2(NO3)4, from UO2(NO3)2·6H2O and KAu(CN)2 is described. The structure contains a three-dimensional (3D) lattice of planar tetranuclear uranyl–oxo–nitrate clusters connected by dicyanoaurate linkers, with the rotation of the clusters providing the increased dimensionality. The material undergoes a reversible single-crystal to single-crystal transformation on exposure to water vapour, which is taken up in the channels of the 3D system. A second uranyl dicyanoaurate coordination polymer of the form [UO2(DMSO)3(H2O)(Au(CN)2)][Au(CN)2] was structurally characterized as a linear chain of dicyanoaurate units connected by gold–gold bonds with pendant uranyl–water–DMSO adducts that are hydrogen bonded into a two-dimensional sheet. Both materials exhibit emission arising from both the uranyl moiety and the gold(I) centre and represent the first multidimensional uranyl–dicyanoaurate coordination polymers.


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